Megalocornea, also known as congenital anterior megalophthalmia, is related to neonatal marfan syndrome and vitreous syneresis. An important gene associated with Megalocornea is CHRDL1 (Chordin Like 1), and among its related pathways/superpathways are Phospholipase-C Pathway and Extracellular matrix organization. Affiliated tissues include eye and endothelial, and related phenotypes are retinal detachment and reduced visual acuity